Synthesis of extended uridine phosphonates derived from an allosteric p2y2 receptor ligand

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Abstract

In this study we report the synthesis of C5/C6-fused uridine phosphonates that are structurally related to earlier reported allosteric P2Y2 receptor ligands. A silyl-Hilbert- Johnson reaction of six quinazoline-2,4-(1H, 3H)-dione-like base moieties with a suitable ribofuranosephosphonate afforded the desired analogues after full deprotection. In contrast to the parent 5-(4-fluoropheny)uridine phosphonate, the present extended-base uridine phosphonates essentially failed to modulate the P2Y2 receptor. © 2014 by the authors; licensee MDPI, Basel, Switzerland.

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Song, L., Risseeuw, M. D. P., Karalic, I., Barrett, M. O., Brown, K. A., Harden, T. K., & Van Calenbergh, S. (2014). Synthesis of extended uridine phosphonates derived from an allosteric p2y2 receptor ligand. Molecules, 19(4), 4313–4325. https://doi.org/10.3390/molecules19044313

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